MA32900B1 - Compose d'aminopyrazole - Google Patents

Compose d'aminopyrazole

Info

Publication number
MA32900B1
MA32900B1 MA33943A MA33943A MA32900B1 MA 32900 B1 MA32900 B1 MA 32900B1 MA 33943 A MA33943 A MA 33943A MA 33943 A MA33943 A MA 33943A MA 32900 B1 MA32900 B1 MA 32900B1
Authority
MA
Morocco
Prior art keywords
aminoprazole
compound
glioblastoma
leukemia
treatment
Prior art date
Application number
MA33943A
Other languages
Arabic (ar)
English (en)
Inventor
Timothy Paul Burkholder
Joshua Ryan Clayton
Liandong Ma
Original Assignee
Lilly Co Eli
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=41630090&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA32900(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Lilly Co Eli filed Critical Lilly Co Eli
Publication of MA32900B1 publication Critical patent/MA32900B1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/5025Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Biomedical Technology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Hematology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

La présente invention porte sur des composés amino pyrazole utiles dans le traitement de troubles myéloprolifératifs chroniques et de divers cancers, par exemple, un glioblastome, un cancer du sein, un myélome multiple, un cancer de la prostate et des leucémies.
MA33943A 2008-12-16 2011-06-14 Compose d'aminopyrazole MA32900B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US12285408P 2008-12-16 2008-12-16
PCT/US2009/067056 WO2010074947A1 (fr) 2008-12-16 2009-12-08 Composé amino pyrazole

Publications (1)

Publication Number Publication Date
MA32900B1 true MA32900B1 (fr) 2011-12-01

Family

ID=41630090

Family Applications (1)

Application Number Title Priority Date Filing Date
MA33943A MA32900B1 (fr) 2008-12-16 2011-06-14 Compose d'aminopyrazole

Country Status (39)

Country Link
US (2) US20100286139A1 (fr)
EP (1) EP2379557B1 (fr)
JP (1) JP5509217B2 (fr)
KR (1) KR101300458B1 (fr)
CN (1) CN102232075B (fr)
AR (1) AR074240A1 (fr)
AU (1) AU2009330503B2 (fr)
BR (1) BRPI0923048A2 (fr)
CA (1) CA2744714C (fr)
CL (1) CL2011001445A1 (fr)
CO (1) CO6331442A2 (fr)
CR (1) CR20110341A (fr)
CY (1) CY1113637T1 (fr)
DK (1) DK2379557T3 (fr)
DO (1) DOP2011000190A (fr)
EA (1) EA019554B1 (fr)
EC (1) ECSP11011132A (fr)
ES (1) ES2396617T3 (fr)
HK (1) HK1160109A1 (fr)
HN (1) HN2011001697A (fr)
HR (1) HRP20120918T1 (fr)
IL (1) IL213065A0 (fr)
JO (1) JO2833B1 (fr)
MA (1) MA32900B1 (fr)
MX (1) MX2011006441A (fr)
MY (1) MY158691A (fr)
NZ (1) NZ592641A (fr)
PA (1) PA8851101A1 (fr)
PE (1) PE20110549A1 (fr)
PL (1) PL2379557T3 (fr)
PT (1) PT2379557E (fr)
SG (1) SG172202A1 (fr)
SI (1) SI2379557T1 (fr)
SV (1) SV2011003949A (fr)
TN (1) TN2011000292A1 (fr)
TW (1) TWI440640B (fr)
UA (1) UA104743C2 (fr)
WO (1) WO2010074947A1 (fr)
ZA (1) ZA201103942B (fr)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2435646A (en) * 2006-03-01 2007-09-05 Spin Tec Engineering Gmbh Apparatus and method of extraction of an arthropod gland
US8105633B2 (en) * 2006-03-01 2012-01-31 Spintec Engineering Gmbh Method and apparatus for extraction of arthropod gland
US20110121485A1 (en) * 2006-10-30 2011-05-26 Spintec Engineering Gmbh Method and apparatus for the manufacture of a fiber
KR20130131461A (ko) * 2011-03-07 2013-12-03 폰다지오네 텔레톤 Tfeb 변종 및 그의 용도
RU2014101070A (ru) * 2011-06-15 2015-07-20 Лайф Энд Брэйн Гмбх Ингибирующие глиобластому соединения и их применение
MX367055B (es) 2012-06-26 2019-08-02 Del Mar Pharmaceuticals El uso de una composición que comprende dianhidrogalactitol, diacetildianhidrogalactitol, y dibromodulcitol, y análogos o derivados de cada uno para el tratamiento de malignidades resistentes a inhibidores de tirosina cinasa.
PL400213A1 (pl) 2012-08-01 2014-02-03 Celon Pharma Spólka Z Ograniczona Odpowiedzialnoscia Pochodne imidazo[1,2-b]pirydazyno-6-aminy jako inhibitory kinazy JAK-2
LT3179991T (lt) 2014-08-11 2021-11-10 Acerta Pharma B.V. Terapiniai btk inhibitoriaus ir bcl-2 inhibitoriaus deriniai
TW201618773A (zh) 2014-08-11 2016-06-01 艾森塔製藥公司 Btk抑制劑、pi3k抑制劑、jak-2抑制劑、及/或cdk4/6抑制劑的治療組合物
WO2016024231A1 (fr) 2014-08-11 2016-02-18 Acerta Pharma B.V. Combinaisons thérapeutiques d'un inhibiteur de btk, d'un inhibiteur de pi3k, d'un inhibiteur de jak-2, d'un inhibiteur de pd-1 et/ou d'un inhibiteur de pd-l1
WO2018093968A1 (fr) * 2016-11-17 2018-05-24 Bristol-Myers Squibb Company Modulateurs d'imidazopyridazine d'il-12, il-23 et/ou ifn-alpha
WO2018167283A1 (fr) 2017-03-17 2018-09-20 INSERM (Institut National de la Santé et de la Recherche Médicale) Procédés pour le diagnostic et le traitement d'un remodelage neuronal associé à un adénocarcinome canalaire pancréatique
US20200088732A1 (en) 2017-04-13 2020-03-19 INSERM (Institut National de la Santé et de la Recherche Mèdicale) Methods for the diagnosis and treatment of pancreatic ductal adenocarcinoma
WO2020092015A1 (fr) 2018-11-02 2020-05-07 University Of Rochester Atténuation thérapeutique d'une infection épithéliale
CN110305140B (zh) 2019-07-30 2020-08-04 上海勋和医药科技有限公司 二氢吡咯并嘧啶类选择性jak2抑制剂

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE326462T1 (de) 2000-12-21 2006-06-15 Vertex Pharma Pyrazolverbindungen als protein-kinase- inhibitoren
JP2003137785A (ja) * 2001-08-23 2003-05-14 Takeda Chem Ind Ltd Jnk活性化阻害剤
AU2002357379A1 (en) 2001-12-21 2003-07-15 Anormed Inc. Chemokine receptor binding heterocyclic compounds with enhanced efficacy
ES2308731T3 (es) 2005-02-16 2008-12-01 Astrazeneca Ab Compuestos quimicos.
ATE473975T1 (de) 2005-02-16 2010-07-15 Astrazeneca Ab Chemische verbindungen
CN101213192B (zh) * 2005-07-01 2012-06-06 Irm责任有限公司 作为蛋白激酶抑制剂的嘧啶取代的苯并咪唑衍生物
GB0515026D0 (en) * 2005-07-21 2005-08-31 Novartis Ag Organic compounds
CA2624882C (fr) * 2005-10-06 2014-05-20 Schering Corporation Pyrazolopyrimidines en tant qu'inhibiteurs de proteines kinases
TWI333953B (en) * 2005-10-06 2010-12-01 Schering Corp Pyrazolopyrimidines as protein kinase inhibitors
AU2006320580B2 (en) 2005-11-30 2011-06-23 Vertex Pharmaceuticals Incorporated Inhibitors of c-Met and uses thereof
US7989459B2 (en) * 2006-02-17 2011-08-02 Pharmacopeia, Llc Purinones and 1H-imidazopyridinones as PKC-theta inhibitors
WO2008030579A2 (fr) 2006-09-07 2008-03-13 Biogen Idec Ma Inc. Modulateurs de la kinase associée au récepteur de l'interleukine-1
CA2667962A1 (fr) * 2006-10-30 2008-05-08 Novartis Ag Composes heterocycliques en tant qu'agents anti-inflammatoires
JP2010524911A (ja) * 2007-04-18 2010-07-22 アストラゼネカ アクチボラグ 5−アミノピラゾール−3−イル−3H−イミダゾ[4,5−b]ピリジン誘導体と癌の治療のためのその使用
CA2686485A1 (fr) 2007-05-23 2008-11-27 Pharmacopeia, Llc Purinones et 1h-imidazopyridinones en tant qu'inhibiteurs de pkc-theta
WO2009062059A2 (fr) 2007-11-08 2009-05-14 Pharmacopeia, Inc. Purinones et 1h-imidazopyridinones isomères comme inhibiteurs de pkc-thêta

Also Published As

Publication number Publication date
KR20110084993A (ko) 2011-07-26
JP5509217B2 (ja) 2014-06-04
SI2379557T1 (sl) 2013-02-28
US20100286139A1 (en) 2010-11-11
TN2011000292A1 (en) 2012-12-17
NZ592641A (en) 2013-01-25
ES2396617T3 (es) 2013-02-22
HK1160109A1 (en) 2012-08-10
DOP2011000190A (es) 2011-07-31
CR20110341A (es) 2011-07-13
PL2379557T3 (pl) 2013-03-29
IL213065A0 (en) 2011-07-31
TWI440640B (zh) 2014-06-11
TW201024301A (en) 2010-07-01
AU2009330503B2 (en) 2012-06-07
WO2010074947A1 (fr) 2010-07-01
MX2011006441A (es) 2011-07-19
US20100152181A1 (en) 2010-06-17
CY1113637T1 (el) 2016-06-22
EA201170831A1 (ru) 2011-12-30
SG172202A1 (en) 2011-07-28
JO2833B1 (en) 2014-09-15
AR074240A1 (es) 2011-01-05
PA8851101A1 (es) 2010-07-27
BRPI0923048A2 (pt) 2018-09-25
PT2379557E (pt) 2013-01-14
CN102232075B (zh) 2013-12-11
SV2011003949A (es) 2011-07-21
AU2009330503A1 (en) 2010-07-01
CO6331442A2 (es) 2011-10-20
EP2379557A1 (fr) 2011-10-26
JP2012512158A (ja) 2012-05-31
ECSP11011132A (es) 2011-07-29
EA019554B1 (ru) 2014-04-30
EP2379557B1 (fr) 2012-10-31
CN102232075A (zh) 2011-11-02
US7897600B2 (en) 2011-03-01
HRP20120918T1 (hr) 2012-12-31
CA2744714C (fr) 2013-06-25
UA104743C2 (ru) 2014-03-11
KR101300458B1 (ko) 2013-08-30
PE20110549A1 (es) 2011-08-04
MY158691A (en) 2016-10-31
HN2011001697A (es) 2013-11-26
ZA201103942B (en) 2012-08-29
CL2011001445A1 (es) 2011-11-11
CA2744714A1 (fr) 2010-07-01
DK2379557T3 (da) 2012-12-17

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